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NCT05058651Toboroz2/3. fázis

Evaluating the Addition of the Immunotherapy Drug Atezolizumab to Standard Chemotherapy Treatment for Advanced or Metastatic Neuroendocrine Carcinomas That Originate Outside the Lung

Randomized Phase II/III Trial of First Line Platinum/Etoposide With or Without Atezolizumab (NSC#783608) in Patients With Advanced or Metastatic Poorly Differentiated Extrapulmonary Neuroendocrine Carcinomas (NEC)

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. nov. 6.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

This phase II/III trial compares the effect of immunotherapy with atezolizumab in combination with standard chemotherapy with a platinum drug (cisplatin or carboplatin) and etoposide versus standard therapy alone for the treatment of poorly differentiated extrapulmonary (originated outside the lung) neuroendocrine cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) or that has spread from where it first started (primary site) to other places in the body (metastatic). The other aim of this trial is to compare using atezolizumab just at the beginning of treatment versus continuing it beyond the initial treatment. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Cisplatin and carboplatin are in a class of medications known as platinum-containing compounds that work by killing, stopping or slowing the growth of cancer cells. Etoposide is in a class of medications known as podophyllotoxin derivatives. It blocks a certain enzyme needed for cell division and DNA repair, and it may kill cancer cells. Giving atezolizumab in combination with a platinum drug (cisplatin or carboplatin) and etoposide may work better in treating patients with poorly differentiated extrapulmonary neuroendocrine cancer compared to standard therapy with a platinum drug (cisplatin or carboplatin) and etoposide alone.

Állapot (regiszter)
Toboroz
Fázis (regiszter)
2/3. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
189 (tervezett)
Első benyújtás
2021. szept. 25.
Kezdés
2022. jún. 28.
Elsődleges befejezés
2028. okt. 1.
Fő szponzor
National Cancer Institute (NCI)
NCT-szám
NCT05058651

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 2/3. fázis
  • Tervezett résztvevők: 189
  • 2022. jún. 28. és az elsődleges befejezés (2028. okt. 1.) között
  • 266 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Kiket keres a vizsgálat

  • Participants must have histologically-confirmed (local site pathological confirmation sufficient) extrapulmonary poorly differentiated, neuroendocrine carcinoma (NEC)
  • Participants must have disease that is unresectable or metastatic and not eligible for definitive therapy as deemed per the treating investigator
  • Participants must have radiologically evaluable disease, measurable or non-measurable, per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria. All measurable and nonmeasurable lesions must be assessed by CT scan with IV contrast of the chest/abdomen/and pelvis (or CT chest without contrast and MRI abdomen/pelvis with gadolinium contrast, if contraindication to CT iodinated contrast) within 28 days prior to registration. While may be used for routine clinical evaluation, PET scans and bone scans alone are not acceptable for disease assessment while participating in this study. All known sites of disease must be assessed and documented on the Baseline Tumor Assessment Form
  • Participants must have brain MRI (or CT head with contrast if there is contraindication to MRI brain) if clinically indicated within 28 days prior to registration. Note: Brain imaging is not required in participants without known and/or clinical concern for brain metastases. Participants with asymptomatic central nervous system (CNS) metastases are eligible if one or more of the following apply:
    • Participants who have received treatment for brain metastases must have:
    • No evidence of radiological progression (by MRI brain or CT head with contrast if there is contraindication to MRI brain) within 28 days prior to registration
    • Discontinued all corticosteroids at least 14 days prior to registration
    • Participants with treatment-naive brain lesions must have:
    • No lesion measuring > 2.0 cm in size in any axis
    • MRI brain or CT head with contrast (if there is contraindication to MRI brain) demonstrating no evidence for mass effect, edema, or other impending neurological compromise within 28 days prior to registration
    • No evidence of radiological progression (by MRI brain or CT head with contrast if there is contraindication to MRI brain) within 28 days prior to registration
    • No need for > 2 mg of dexamethasone (or equivalent of > 10 mg prednisone) per day at time of registration
  • Participants must not have symptomatic central nervous system (CNS) metastases
  • Participants must not have known or suspected leptomeningeal disease
  • Participants with prior history of non-metastatic (localized/locally advanced disease) extrapulmonary poorly differentiated NEC may have had prior platinum-based therapy +/- radiation +/- surgery provided that all therapy was completed >= 6 months prior to registration
  • Participants must discontinue denosumab prior to study registration and plan to replace with a bisphosphonate while on the study
  • Participants must not have had prior treatment for advanced or metastatic NEC EXCEPT one cycle of platinum (carboplatin/cisplatin) + etoposide is allowed prior to registration. Other chemotherapy regimens are not allowed. For participants with prostate or urothelial NEC, prior chemotherapy for the non-NEC component (e.g. adenocarcinoma or urothelial) is allowed as long as such therapy was completed >= 24 weeks prior to registration and participants have recovered from all prior toxicities to =< grade 1.
  • Participants must not have had prior treatment with an anti-PD-1, anti-PD-L1, antiPD-L2, CD137 agonists, anti-CTLA-4 agent, or any other immune checkpoint inhibitors for any neuroendocrine neoplasm. Immune checkpoint inhibitors given for other cancer indications are allowed provided last therapy was given at least 12 months prior to study registration
  • Participants must not have received treatment with systemic immunostimulatory agents including, but not limited to, interferon and interleukin2 [IL-2] within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to registration
  • Participants must not have had history of known severe allergy, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies, including to Chinese hamster ovary cell products or to any component of the atezolizumab formulation, cisplatin, carboplatin, or etoposide
  • Participants must not be on active systemic therapy for another cancer with the exception of hormonal therapy including androgen deprivation therapy (e.g., gonadotropin-releasing hormone [GnRH] agonists or antagonists), which can be continued while participants are receiving protocol therapy. Use of enzalutamide or apalutamide is permitted after completion of chemotherapy and must be held during chemotherapy for participants receiving prior to enrollment. Use of darolutamide is permitted during chemotherapy. Glucocorticoid-containing regimens, including abiraterone, are not permitted.
  • Participants must be >= 18 years of age
  • Participants must have a Zubrod performance status of =< 2 within 28 days prior to registration
  • Participants must have a complete medical history and physical exam within 28 days prior to registration
  • Absolute neutrophil count (ANC) >= 1.5 x 10\^9 /L (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Hemoglobin >= 9.0 g/dl (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Platelet count >= 100 x 10\^9/L (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 2.5 x institutional upper limit of normal (ULN) (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Serum total bilirubin =< 1.5 x ULN (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Adequate renal function as defined by any 1 of the following: 1) Measured creatinine clearance (CL) > 50 mL/min OR 2) Calculated creatinine CL > 50 mL/min by the Cockcroft-Gault formula OR by 24-hour urine collection for determination of creatinine clearance (obtained within 14 days prior to registration. For participants who received a cycle of chemotherapy prior to registration, at least 21 days must have elapsed between day 1 of platinum + etoposide and performance of these tests)
  • Participants must not have uncontrolled or symptomatic hypercalcemia (> 1.5 mmol/L ionized calcium or calcium > 12 mg/dL or corrected serum calcium > ULN) within 14 days prior to registration. Participants who have asymptomatic hypercalcemia are eligible provided that medical therapy to treat the hypercalcemia is planned
  • Participants must not have a diagnosis of immunodeficiency nor be receiving systemic steroid therapy (equivalent of > 20 mg of hydrocortisone per day) or any other form of immunosuppressive therapy within 14 days prior to registration
  • Participants must not have active or history of autoimmune disease or immune deficiency, including, but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid antibody syndrome, Wegener granulomatosis, Sjogren syndrome, Guillain-Barre syndrome, or multiple sclerosis with the following exceptions:
    • Patients with a history of autoimmune-related hypothyroidism who are on thyroid-replacement hormone are eligible for the study
    • Patients with controlled type 1 diabetes mellitus who are on an insulin regimen are eligible for the study
    • Patients with eczema, psoriasis, lichen simplex chronicus, or vitiligo with dermatologic manifestations only (e.g., patients with psoriatic arthritis are excluded) are eligible for the study provided all of following conditions are met:
    • Rash must cover < 10% of body surface area
    • Disease is well controlled at baseline and requires only low-potency topical corticosteroids
    • No occurrence of acute exacerbations of the underlying condition requiring psoralen plus ultraviolet A radiation, methotrexate, retinoids, biologic agents, oral calcineurin inhibitors, or high-potency or oral corticosteroids within the previous 12 months
  • Participants must not have history of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan. NOTE: History of radiation pneumonitis in the radiation field (fibrosis) is permitted
  • Participants must not have significant cardiovascular disease, such as New York Heart Association class II or greater cardiac disease, myocardial infarction within 3 months prior to registration, unstable arrythmias, or unstable angina
  • Participants must not have had a major surgical procedure other than for diagnosis within 28 days prior to registration. Participant must not plan to receive a major surgical procedure during the course of protocol treatment. NOTE: Patient port placement is not considered a major surgery
  • Participants must not have severe infections (i.e., Common Terminology Criteria for Adverse Events [CTCAE] grade >= 2) at time of registration, including but not limited to hospitalization for complications for infection, bacteremia, or severe pneumonia
  • Participants must not have known active tuberculosis
  • Participants with evidence of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load, with testing performed as clinically indicated
  • Participants with a history of hepatitis C virus (HCV) infection must have been treated and cured. Participants with active HCV infection who are currently on treatment must have an undetectable HCV viral load, with testing performed as clinically indicated
  • Participants with known human immunodeficiency virus (HIV)-infection must be on effective anti-retroviral therapy at time of registration and have undetectable HIV viral load within 6 months of registration
  • Participants must not have prior allogeneic bone marrow transplantation or solid organ transplant
  • Participants must not have received administration of a live, attenuated vaccine (e.g., FluMist [registered trademark]) within 28 days prior to initiation of study treatment, during treatment with atezolizumab, and not plan to receive for 5 months after the last dose of atezolizumab
  • Participants must not be pregnant due to the possibility of harm to the fetus. Individuals who are of reproductive potential must have agreed to use an effective contraceptive method (with details provided as a part of the consent process) during the treatment period and for 5 months after the final dose of atezolizumab. A person who has had menses at any time in the preceding 12 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen
  • Participants must be offered the opportunity to participate in specimen banking. With participant consent, specimens must be collected and submitted via the Southwest Oncology Group (SWOG) Specimen Tracking System
  • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines

Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (266)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Hawaii Cancer Care - Westridge‘AieaEgyesült ÁllamokToboroz
Pali Momi Medical Center‘AieaEgyesült ÁllamokFelfüggesztve
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McFarland Clinic - AmesAmesEgyesült ÁllamokToboroz
Community Hospital of AnacondaAnacondaEgyesült ÁllamokToboroz
Kaiser Permanente-AnaheimAnaheimEgyesült ÁllamokToboroz
Alaska Women's Cancer CareAnchorageEgyesült ÁllamokFelfüggesztve
UI Health Care Mission Cancer and Blood - Ankeny ClinicAnkenyEgyesült ÁllamokToboroz
Trinity Health Saint Joseph Mercy Hospital Ann ArborAnn ArborEgyesült ÁllamokToboroz
University of Michigan Rogel Cancer CenterAnn ArborEgyesült ÁllamokToboroz
Sutter Auburn Faith HospitalAuburnEgyesült ÁllamokToboroz
Sutter Cancer Centers Radiation Oncology Services-AuburnAuburnEgyesült ÁllamokToboroz
Rush-Copley Medical CenterAuroraEgyesült ÁllamokFelfüggesztve
Kaiser Permanente-Baldwin ParkBaldwin ParkEgyesült ÁllamokToboroz
LSU Health Baton Rouge-North ClinicBaton RougeEgyesült ÁllamokToboroz
Our Lady of the Lake Physician GroupBaton RougeEgyesült ÁllamokToboroz
Bronson Battle CreekBattle CreekEgyesült ÁllamokToboroz
Kaiser Permanente-BellflowerBellflowerEgyesült ÁllamokToboroz
Saint Charles Health SystemBendEgyesült ÁllamokToboroz
Alta Bates Summit Medical Center-Herrick CampusBerkeleyEgyesült ÁllamokToboroz
Saint Vincent Frontier Cancer CenterBillingsEgyesült ÁllamokToboroz
Billings Clinic Cancer CenterBillingsEgyesült ÁllamokToboroz
McFarland Clinic - BooneBooneEgyesült ÁllamokFelfüggesztve
United Hospital CenterBridgeportEgyesült ÁllamokToboroz
Trinity Health IHA Medical Group Hematology Oncology - BrightonBrightonEgyesült ÁllamokToboroz
Trinity Health Medical Center - BrightonBrightonEgyesült ÁllamokToboroz
Henry Ford Cancer Institute-DownriverBrownstownEgyesült ÁllamokToboroz
Roswell Park Cancer InstituteBuffaloEgyesült ÁllamokFut, nem toboroz
Lahey ClinicBurlingtonEgyesült ÁllamokToboroz
Minnesota Oncology - BurnsvilleBurnsvilleEgyesült ÁllamokToboroz
Sutter Cancer Centers Radiation Oncology Services-Cameron ParkCameron ParkEgyesült ÁllamokToboroz
Trinity Health Medical Center - CantonCantonEgyesült ÁllamokToboroz
Trinity Health IHA Medical Group Hematology Oncology - CantonCantonEgyesült ÁllamokToboroz
Saint Francis Medical CenterCape GirardeauEgyesült ÁllamokToboroz
Mercy San Juan Medical CenterCarmichaelEgyesült ÁllamokToboroz
Mercy Cancer Center - CarmichaelCarmichaelEgyesült ÁllamokToboroz
Saint Anthony Regional HospitalCarrollEgyesült ÁllamokToboroz
Duke Cancer Center CaryCaryEgyesült ÁllamokFelfüggesztve
Centralia Oncology ClinicCentraliaEgyesült ÁllamokToboroz
WellSpan Medical Oncology and HematologyChambersburgEgyesült ÁllamokToboroz
Medical University of South CarolinaCharlestonEgyesült ÁllamokFelfüggesztve
Atrium Health Pineville/LCI-PinevilleCharlotteEgyesült ÁllamokToboroz
Carolinas Medical Center/Levine Cancer InstituteCharlotteEgyesült ÁllamokToboroz
Levine Cancer Institute-BallantyneCharlotteEgyesült ÁllamokToboroz
Atrium Health University City/LCI-UniversityCharlotteEgyesült ÁllamokToboroz
Levine Cancer Institute-SouthParkCharlotteEgyesült ÁllamokToboroz
Trinity Health IHA Medical Group Hematology Oncology - Chelsea HospitalChelseaEgyesült ÁllamokToboroz
Chelsea HospitalChelseaEgyesült ÁllamokToboroz
Northwestern UniversityChicagoEgyesült ÁllamokToboroz
University of Chicago Comprehensive Cancer CenterChicagoEgyesült ÁllamokToboroz
Providence Cancer Institute Clackamas ClinicClackamasEgyesült ÁllamokFelfüggesztve
Southeastern Medical Oncology Center-ClintonClintonEgyesült ÁllamokToboroz
Henry Ford Macomb Hospital-Clinton TownshipClinton TownshipEgyesült ÁllamokToboroz
UI Health Care Mission Cancer and Blood - West Des Moines ClinicCliveEgyesült ÁllamokToboroz
Mercy Cancer Center-West LakesCliveEgyesült ÁllamokToboroz
Kootenai Health - Coeur d'AleneCoeur d'AleneEgyesült ÁllamokToboroz
Ohio State University Comprehensive Cancer CenterColumbusEgyesült ÁllamokToboroz
Atrium Health Cabarrus/LCI-ConcordConcordEgyesült ÁllamokToboroz
Greater Regional Medical CenterCrestonEgyesült ÁllamokFut, nem toboroz
UChicago Medicine Northwest IndianaCrown PointEgyesült ÁllamokToboroz
Parkland Memorial HospitalDallasEgyesült ÁllamokToboroz
UT Southwestern Simmons Cancer Center - RedBirdDallasEgyesült ÁllamokToboroz
UT Southwestern/Simmons Cancer Center-DallasDallasEgyesült ÁllamokToboroz
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Henry Ford Medical Center-FairlaneDearbornEgyesült ÁllamokToboroz
Corewell Health Dearborn HospitalDearbornEgyesült ÁllamokToboroz
Cancer Care Specialists of Illinois - DecaturDecaturEgyesült ÁllamokToboroz
Decatur Memorial HospitalDecaturEgyesült ÁllamokToboroz
Northwestern Medicine Cancer Center KishwaukeeDeKalbEgyesült ÁllamokToboroz
AdventHealth PorterDenverEgyesült ÁllamokToboroz
Smilow Cancer Hospital-Derby Care CenterDerbyEgyesült ÁllamokToboroz
UI Health Care Mission Cancer and Blood - Des Moines ClinicDes MoinesEgyesült ÁllamokToboroz
Broadlawns Medical CenterDes MoinesEgyesült ÁllamokToboroz
Mercy Medical Center - Des MoinesDes MoinesEgyesült ÁllamokToboroz
UI Health Care Mission Cancer and Blood - Laurel ClinicDes MoinesEgyesült ÁllamokToboroz
Iowa Methodist Medical CenterDes MoinesEgyesült ÁllamokToboroz
Wayne State University/Karmanos Cancer InstituteDetroitEgyesült ÁllamokFut, nem toboroz
Henry Ford HospitalDetroitEgyesült ÁllamokToboroz
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Fairview Southdale HospitalEdinaEgyesült ÁllamokToboroz
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Crossroads Cancer CenterEffinghamEgyesült ÁllamokToboroz
Carle Physician Group-EffinghamEffinghamEgyesült ÁllamokToboroz
Mercy Cancer Center - Elk GroveElk GroveEgyesült ÁllamokToboroz
Ephrata Cancer CenterEphrataEgyesült ÁllamokToboroz
The Queen's Medical Center - West Oahu‘Ewa BeachEgyesült ÁllamokToboroz
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Holy Cross HospitalFort LauderdaleEgyesült ÁllamokToboroz
UT Southwestern/Simmons Cancer Center-Fort WorthFort WorthEgyesült ÁllamokToboroz
Palo Alto Medical Foundation-FremontFremontEgyesült ÁllamokToboroz
Levine Cancer Institute-GastonGastoniaEgyesült ÁllamokToboroz
Northwestern Medicine Cancer Center DelnorGenevaEgyesült ÁllamokToboroz
Adams Cancer CenterGettysburgEgyesült ÁllamokToboroz
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Northwestern Medicine Glenview Outpatient CenterGlenviewEgyesült ÁllamokToboroz
Southeastern Medical Oncology Center-GoldsboroGoldsboroEgyesült ÁllamokToboroz
Trinity Health Grand Rapids HospitalGrand RapidsEgyesült ÁllamokToboroz
Corewell Health Grand Rapids Hospitals - Butterworth HospitalGrand RapidsEgyesült ÁllamokToboroz
Northwestern Medicine Grayslake Outpatient CenterGrayslakeEgyesült ÁllamokToboroz
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Smilow Cancer Hospital Care Center at GreenwichGreenwichEgyesült ÁllamokToboroz
Henry Ford Saint John Hospital - Van ElslanderGrosse Pointe WoodsEgyesült ÁllamokToboroz
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Henry Ford Saint John Hospital - BreastGrosse Pointe WoodsEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center - GuilfordGuilfordEgyesült ÁllamokToboroz
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Kaiser Permanente South BayHarbor CityEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center at Saint FrancisHartfordEgyesült ÁllamokFelfüggesztve
Ingalls Memorial HospitalHarveyEgyesült ÁllamokToboroz
University of Hawaii Cancer CenterHonoluluEgyesült ÁllamokToboroz
Queen's Cancer Center - KuakiniHonoluluEgyesült ÁllamokToboroz
Queen's Medical CenterHonoluluEgyesült ÁllamokToboroz
Straub Clinic and HospitalHonoluluEgyesült ÁllamokToboroz
Queen's Cancer Cenrer - POB IHonoluluEgyesült ÁllamokToboroz
Hawaii Cancer Care Inc - Waterfront PlazaHonoluluEgyesült ÁllamokToboroz
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer CenterHoustonEgyesült ÁllamokToboroz
Ben Taub General HospitalHoustonEgyesült ÁllamokToboroz
Kaiser Permanente-IrvineIrvineEgyesült ÁllamokToboroz
Allegiance HealthJacksonEgyesült ÁllamokToboroz
Mayo Clinic in FloridaJacksonvilleEgyesült ÁllamokToboroz
Southeastern Medical Oncology Center-JacksonvilleJacksonvilleEgyesült ÁllamokToboroz
McFarland Clinic - JeffersonJeffersonEgyesült ÁllamokFelfüggesztve
Mercy Hospital JoplinJoplinEgyesült ÁllamokToboroz
West Michigan Cancer CenterKalamazooEgyesült ÁllamokToboroz
Bronson Methodist HospitalKalamazooEgyesült ÁllamokToboroz
Logan Health Medical CenterKalispellEgyesült ÁllamokToboroz
Gundersen Lutheran Medical CenterLa CrosseEgyesült ÁllamokToboroz
Northwestern Medicine Lake Forest HospitalLake ForestEgyesült ÁllamokToboroz
Karmanos Cancer Institute at McLaren Greater LansingLansingEgyesült ÁllamokFut, nem toboroz
Cancer Centers of Southwest Oklahoma ResearchLawtonEgyesült ÁllamokToboroz
Dartmouth Hitchcock Medical Center/Dartmouth Cancer CenterLebanonEgyesült ÁllamokToboroz
Sechler Family Cancer CenterLebanonEgyesült ÁllamokToboroz
AdventHealth LittletonLittletonEgyesült ÁllamokToboroz
Trinity Health Saint Mary Mercy Livonia HospitalLivoniaEgyesült ÁllamokToboroz
Kaiser Permanente West Los AngelesLos AngelesEgyesült ÁllamokToboroz
Kaiser Permanente Los Angeles Medical CenterLos AngelesEgyesült ÁllamokToboroz
Henry Ford Warren Hospital - Breast MacombMacombEgyesült ÁllamokToboroz
Henry Ford Saint John Hospital - Macomb MedicalMacombEgyesült ÁllamokToboroz
McFarland Clinic - MarshalltownMarshalltownEgyesült ÁllamokToboroz
Marshfield Medical Center-MarshfieldMarshfieldEgyesült ÁllamokToboroz
Carle Physician Group-Mattoon/CharlestonMattoonEgyesült ÁllamokToboroz
East Jefferson General HospitalMetairieEgyesült ÁllamokToboroz
LSU Healthcare Network / Metairie Multi-Specialty ClinicMetairieEgyesült ÁllamokToboroz
Medical College of WisconsinMilwaukeeEgyesült ÁllamokToboroz
Hennepin County Medical CenterMinneapolisEgyesült ÁllamokToboroz
Abbott-Northwestern HospitalMinneapolisEgyesült ÁllamokToboroz
Marshfield Medical Center - MinocquaMinocquaEgyesült ÁllamokToboroz
Community Medical CenterMissoulaEgyesült ÁllamokToboroz
Memorial Medical CenterModestoEgyesült ÁllamokToboroz
West Virginia University HealthcareMorgantownEgyesült ÁllamokToboroz
Palo Alto Medical Foundation-Camino DivisionMountain ViewEgyesült ÁllamokToboroz
SSM Health Good SamaritanMount VernonEgyesült ÁllamokToboroz
Trinity Health Muskegon HospitalMuskegonEgyesült ÁllamokToboroz
Saint Alphonsus Cancer Care Center-NampaNampaEgyesült ÁllamokToboroz
Vanderbilt University/Ingram Cancer CenterNashvilleEgyesült ÁllamokToboroz
Providence Newberg Medical CenterNewbergEgyesült ÁllamokToboroz
Yale UniversityNew HavenEgyesült ÁllamokToboroz
UC Comprehensive Cancer Center at Silver CrossNew LenoxEgyesült ÁllamokToboroz
University Medical Center New OrleansNew OrleansEgyesült ÁllamokToboroz
Mount Sinai HospitalNew YorkEgyesült ÁllamokFut, nem toboroz
Corewell Health Lakeland Hospitals - Niles HospitalNilesEgyesült ÁllamokToboroz
Carle Cancer Institute NormalNormalEgyesült ÁllamokToboroz
Carle BroMenn Medical CenterNormalEgyesült ÁllamokToboroz
Yale-New Haven Hospital North Haven Medical CenterNorth HavenEgyesült ÁllamokToboroz
Cancer and Hematology Centers of Western Michigan - Norton ShoresNorton ShoresEgyesült ÁllamokFelfüggesztve
Henry Ford Medical Center-ColumbusNoviEgyesült ÁllamokToboroz
Cancer Care Center of O'FallonO'FallonEgyesült ÁllamokToboroz
Mercy Hospital Oklahoma CityOklahoma CityEgyesült ÁllamokToboroz
University of Oklahoma Health Sciences CenterOklahoma CityEgyesült ÁllamokToboroz
Kaiser Permanente-OntarioOntarioEgyesült ÁllamokToboroz
Providence Willamette Falls Medical CenterOregon CityEgyesült ÁllamokToboroz
University of Chicago Medicine-Orland ParkOrland ParkEgyesült ÁllamokToboroz
Northwestern Medicine Orland ParkOrland ParkEgyesült ÁllamokToboroz
Palo Alto Medical Foundation Health CarePalo AltoEgyesült ÁllamokToboroz
Kaiser Permanente - Panorama CityPanorama CityEgyesült ÁllamokToboroz
AdventHealth ParkerParkerEgyesült ÁllamokToboroz
Lahey Clinic PeabodyPeabodyEgyesült ÁllamokToboroz
Cancer Center at Saint Joseph'sPhoenixEgyesült ÁllamokToboroz
Mayo Clinic Hospital in ArizonaPhoenixEgyesült ÁllamokToboroz
FirstHealth of the Carolinas-Moore Regional HospitalPinehurstEgyesült ÁllamokToboroz
Trinity Health Saint Joseph Mercy Oakland HospitalPontiacEgyesült ÁllamokToboroz
Providence Saint Vincent Medical CenterPortlandEgyesült ÁllamokToboroz
Providence Portland Medical CenterPortlandEgyesült ÁllamokToboroz
Kootenai Clinic Cancer Services - Post FallsPost FallsEgyesült ÁllamokToboroz
Duke Cancer Center RaleighRaleighEgyesült ÁllamokToboroz
Rapid City Regional HospitalRapid CityEgyesült ÁllamokToboroz
Corewell Health Reed City HospitalReed CityEgyesült ÁllamokToboroz
Marshfield Medical Center-Rice LakeRice LakeEgyesült ÁllamokToboroz
UT Southwestern Clinical Center at Richardson/PlanoRichardsonEgyesült ÁllamokToboroz
Kaiser Permanente-RiversideRiversideEgyesült ÁllamokToboroz
Mayo Clinic in RochesterRochesterEgyesült ÁllamokToboroz
UW Health Carbone Cancer Center RockfordRockfordEgyesült ÁllamokToboroz
Levine Cancer Institute-Rock HillRock HillEgyesült ÁllamokToboroz
Mercy Cancer Center - RocklinRocklinEgyesült ÁllamokToboroz
Sutter Roseville Medical CenterRosevilleEgyesült ÁllamokToboroz
Sutter Cancer Centers Radiation Oncology Services-RosevilleRosevilleEgyesült ÁllamokToboroz
Corewell Health William Beaumont University HospitalRoyal OakEgyesült ÁllamokToboroz
Mercy Cancer Center - SacramentoSacramentoEgyesült ÁllamokToboroz
Sutter Medical Center SacramentoSacramentoEgyesült ÁllamokToboroz
Dartmouth Cancer Center - NorthSaint JohnsburyEgyesült ÁllamokToboroz
Corewell Health Lakeland Hospitals - Saint Joseph HospitalSaint JosephEgyesült ÁllamokToboroz
Corewell Health Lakeland Hospitals - Marie Yeager Cancer CenterSaint JosephEgyesült ÁllamokToboroz
Park Nicollet Clinic - Saint Louis ParkSaint Louis ParkEgyesült ÁllamokToboroz
United HospitalSaint PaulEgyesült ÁllamokToboroz
Regions HospitalSaint PaulEgyesült ÁllamokToboroz
Huntsman Cancer Institute/University of UtahSalt Lake CityEgyesült ÁllamokToboroz
Kaiser Permanente-San Diego ZionSan DiegoEgyesült ÁllamokToboroz
Kootenai Clinic Cancer Services - SandpointSandpointEgyesült ÁllamokToboroz
California Pacific Medical Center-Pacific CampusSan FranciscoEgyesült ÁllamokToboroz
Kaiser Permanente-San MarcosSan MarcosEgyesült ÁllamokToboroz
Palo Alto Medical Foundation-Santa CruzSanta CruzEgyesült ÁllamokToboroz
Sutter Pacific Medical FoundationSanta RosaEgyesült ÁllamokToboroz
Fred Hutchinson Cancer CenterSeattleEgyesült ÁllamokToboroz
University of Washington Medical Center - MontlakeSeattleEgyesült ÁllamokToboroz
Saint Francis Regional Medical CenterShakopeeEgyesült ÁllamokToboroz
Atrium Health Cleveland/LCI-ClevelandShelbyEgyesült ÁllamokToboroz
CoxHealth South HospitalSpringfieldEgyesült ÁllamokToboroz
Springfield ClinicSpringfieldEgyesült ÁllamokToboroz
Southern Illinois University School of MedicineSpringfieldEgyesült ÁllamokToboroz
Springfield Memorial HospitalSpringfieldEgyesült ÁllamokToboroz
Mercy Hospital SpringfieldSpringfieldEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center at Long RidgeStamfordEgyesült ÁllamokToboroz
Marshfield Medical Center-River Region at Stevens PointStevens PointEgyesült ÁllamokToboroz
Mercy Hospital SouthSt LouisEgyesült ÁllamokToboroz
Stony Brook University Medical CenterStony BrookEgyesült ÁllamokFut, nem toboroz
Palo Alto Medical Foundation-SunnyvaleSunnyvaleEgyesült ÁllamokToboroz
Moffitt Cancer CenterTampaEgyesült ÁllamokToboroz
Toledo Clinic Cancer Centers-ToledoToledoEgyesült ÁllamokFelfüggesztve
Smilow Cancer Hospital-Torrington Care CenterTorringtonEgyesült ÁllamokToboroz
Munson Medical CenterTraverse CityEgyesült ÁllamokToboroz
Corewell Health Beaumont Troy HospitalTroyEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center-TrumbullTrumbullEgyesült ÁllamokToboroz
Carle Cancer CenterUrbanaEgyesült ÁllamokToboroz
Sutter Solano Medical Center/Cancer CenterVallejoEgyesült ÁllamokToboroz
Henry Ford Health Warren HospitalWarrenEgyesült ÁllamokToboroz
Henry Ford Madison Heights Hospital - BreastWarrenEgyesült ÁllamokToboroz
Henry Ford Warren Hospital - GLCMSWarrenEgyesült ÁllamokToboroz
Northwestern Medicine Cancer Center WarrenvilleWarrenvilleEgyesült ÁllamokToboroz
Smilow Cancer Hospital-Waterbury Care CenterWaterburyEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center - WaterfordWaterfordEgyesült ÁllamokToboroz
UI Health Care Mission Cancer and Blood - Waukee ClinicWaukeeEgyesült ÁllamokToboroz
Henry Ford West Bloomfield HospitalWest BloomfieldEgyesült ÁllamokToboroz
Mercy Medical Center-West LakesWest Des MoinesEgyesült ÁllamokToboroz
Smilow Cancer Hospital Care Center - WesterlyWesterlyEgyesült ÁllamokToboroz
Marshfield Medical Center - WestonWestonEgyesült ÁllamokToboroz
Woodland Memorial HospitalWoodlandEgyesült ÁllamokToboroz
Kaiser Permanente-Woodland HillsWoodland HillsEgyesült ÁllamokToboroz
Henry Ford Wyandotte HospitalWyandotteEgyesült ÁllamokToboroz
University of Michigan Health - WestWyomingEgyesült ÁllamokToboroz
WellSpan Health-York Cancer CenterYorkEgyesült ÁllamokToboroz
Cancer Care Associates of YorkYorkEgyesült ÁllamokFelfüggesztve
Rush-Copley Healthcare CenterYorkvilleEgyesült ÁllamokFelfüggesztve
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor CampusYpsilantiEgyesült ÁllamokToboroz
Huron Gastroenterology PCYpsilantiEgyesült ÁllamokToboroz

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